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Bruton's X-linked agammaglobulinemia
Bruton's disease
Bruton's hypogammaglobulinemia
Congenital hypogammaglobulinaemia
Congenital hypogammaglobulinemia
Hypogammaglobulinemia
X-linked agammaglobulinaemia
XLA

Traduction de «Hypogammaglobulinemia » (Anglais → Néerlandais) :



Bruton's disease | Bruton's hypogammaglobulinemia | Bruton's X-linked agammaglobulinemia | X-linked agammaglobulinaemia | XLA [Abbr.]

Bruton hypogamma globulinemie | ziekte van Bruton


congenital hypogammaglobulinaemia | congenital hypogammaglobulinemia

congenitale hypogammaglobulinemie


Syndrome that is characterized by the association of severe hypogammaglobulinemia, combined T and B cell immunodeficiency, absent lymph node germinal centers, absent tissue plasma cells and hepatic veno-occlusive disease. Mutations in the gene coding

hepatische veno-occlusieve ziekte, immuundeficiëntie


A rare genetic endocrine disease characterized by the association of common variable immunodeficiency manifesting with hypogammaglobulinemia and recurrent or severe childhood-onset sinopulmonary infections, followed, possibly many years later, by sym

deficiëntie in anterieure hypofysefunctie, variabele immuundeficiëntiesyndroom




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'Hypogammaglobulinemia' ->

Date index: 2023-03-09
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